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Supplementation with complex milk lipids during brain development promotes neuroplasticity without altering myelination or vascular density

BACKGROUND: Supplementation with complex milk lipids (CML) during postnatal brain development has been shown to improve spatial reference learning in rats. OBJECTIVE: The current study examined histo-biological changes in the brain following CML supplementation and their relationship to the observed...

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Autores principales: Guillermo, Rosamond B., Yang, Panzao, Vickers, Mark H., McJarrow, Paul, Guan, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377325/
https://www.ncbi.nlm.nih.gov/pubmed/25818888
http://dx.doi.org/10.3402/fnr.v59.25765
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author Guillermo, Rosamond B.
Yang, Panzao
Vickers, Mark H.
McJarrow, Paul
Guan, Jian
author_facet Guillermo, Rosamond B.
Yang, Panzao
Vickers, Mark H.
McJarrow, Paul
Guan, Jian
author_sort Guillermo, Rosamond B.
collection PubMed
description BACKGROUND: Supplementation with complex milk lipids (CML) during postnatal brain development has been shown to improve spatial reference learning in rats. OBJECTIVE: The current study examined histo-biological changes in the brain following CML supplementation and their relationship to the observed improvements in memory. DESIGN: The study used the brain tissues from the rats (male Wistar, 80 days of age) after supplementing with either CML or vehicle during postnatal day 10–80. Immunohistochemical staining of synaptophysin, glutamate receptor-1, myelin basic protein, isolectin B-4, and glial fibrillary acidic protein was performed. The average area and the density of the staining and the numbers of astrocytes and capillaries were assessed and analysed. RESULTS: Compared with control rats, CML supplementation increased the average area of synaptophysin staining and the number of GFAP astrocytes in the CA3 sub-region of the hippocampus (p<0.01), but not in the CA4 sub-region. The supplementation also led to an increase in dopamine output in the striatum that was related to nigral dopamine expression (p<0.05), but did not alter glutamate receptors, myelination or vascular density. CONCLUSION: CML supplementation may enhance neuroplasticity in the CA3 sub-regions of the hippocampus. The brain regions-specific increase of astrocyte may indicate a supporting role for GFAP in synaptic plasticity. CML supplementation did not associate with postnatal white matter development or vascular remodelling.
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spelling pubmed-43773252015-04-02 Supplementation with complex milk lipids during brain development promotes neuroplasticity without altering myelination or vascular density Guillermo, Rosamond B. Yang, Panzao Vickers, Mark H. McJarrow, Paul Guan, Jian Food Nutr Res Original Article BACKGROUND: Supplementation with complex milk lipids (CML) during postnatal brain development has been shown to improve spatial reference learning in rats. OBJECTIVE: The current study examined histo-biological changes in the brain following CML supplementation and their relationship to the observed improvements in memory. DESIGN: The study used the brain tissues from the rats (male Wistar, 80 days of age) after supplementing with either CML or vehicle during postnatal day 10–80. Immunohistochemical staining of synaptophysin, glutamate receptor-1, myelin basic protein, isolectin B-4, and glial fibrillary acidic protein was performed. The average area and the density of the staining and the numbers of astrocytes and capillaries were assessed and analysed. RESULTS: Compared with control rats, CML supplementation increased the average area of synaptophysin staining and the number of GFAP astrocytes in the CA3 sub-region of the hippocampus (p<0.01), but not in the CA4 sub-region. The supplementation also led to an increase in dopamine output in the striatum that was related to nigral dopamine expression (p<0.05), but did not alter glutamate receptors, myelination or vascular density. CONCLUSION: CML supplementation may enhance neuroplasticity in the CA3 sub-regions of the hippocampus. The brain regions-specific increase of astrocyte may indicate a supporting role for GFAP in synaptic plasticity. CML supplementation did not associate with postnatal white matter development or vascular remodelling. Co-Action Publishing 2015-03-27 /pmc/articles/PMC4377325/ /pubmed/25818888 http://dx.doi.org/10.3402/fnr.v59.25765 Text en © 2015 Rosamond B. Guillermo et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license.
spellingShingle Original Article
Guillermo, Rosamond B.
Yang, Panzao
Vickers, Mark H.
McJarrow, Paul
Guan, Jian
Supplementation with complex milk lipids during brain development promotes neuroplasticity without altering myelination or vascular density
title Supplementation with complex milk lipids during brain development promotes neuroplasticity without altering myelination or vascular density
title_full Supplementation with complex milk lipids during brain development promotes neuroplasticity without altering myelination or vascular density
title_fullStr Supplementation with complex milk lipids during brain development promotes neuroplasticity without altering myelination or vascular density
title_full_unstemmed Supplementation with complex milk lipids during brain development promotes neuroplasticity without altering myelination or vascular density
title_short Supplementation with complex milk lipids during brain development promotes neuroplasticity without altering myelination or vascular density
title_sort supplementation with complex milk lipids during brain development promotes neuroplasticity without altering myelination or vascular density
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377325/
https://www.ncbi.nlm.nih.gov/pubmed/25818888
http://dx.doi.org/10.3402/fnr.v59.25765
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